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112849-15-7

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112849-15-7 Usage

Chemical Properties

White Solid

Uses

Reactant in the preparation of Vitamin D2 (V676040) derivatives.

Check Digit Verification of cas no

The CAS Registry Mumber 112849-15-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,8,4 and 9 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112849-15:
(8*1)+(7*1)+(6*2)+(5*8)+(4*4)+(3*9)+(2*1)+(1*5)=117
117 % 10 = 7
So 112849-15-7 is a valid CAS Registry Number.

112849-15-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-cyclopropyl-2-oxoethyl)-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names Phosphonium,(2-cyclopropyl-2-oxoethyl)triphenyl-,bromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:112849-15-7 SDS

112849-15-7Downstream Products

112849-15-7Relevant articles and documents

A Ba/Pd Catalytic System Enables Dehydrative Cross-Coupling and Excellent E-Selective Wittig Reactions

Xie, Peizhong,Fu, Weishan,Cai, Xinying,Sun, Zuolian,Wu, Ying,Li, Shuangshuang,Gao, Cuiqing,Yang, Xiaobo,Loh, Teck-Peng

supporting information, p. 7055 - 7059 (2019/09/12)

A Ba/Pd cooperative catalysis system was developed to enable the dehydrative cross-coupling of allylic alcohols with P-ylides to occur directly and promote a subsequent Wittig reaction in one pot. A variety of multisubstituted 1,4-dienes were isolated in good to excellent yields with broad P-ylides (stabilized by both ester and ketone carbonyl groups) and aldehyde (aliphatic and aromatic) substrates with excellent E selectivity.

Synthesis of Polysubstituted Pyridines via a One-Pot Metal-Free Strategy

Wei, Hongbo,Li, Yun,Xiao, Ke,Cheng, Bin,Wang, Huifei,Hu, Lin,Zhai, Hongbin

supporting information, p. 5974 - 5977 (2016/01/09)

An efficient strategy for the one-pot synthesis of polysubstituted pyridines via a cascade reaction from aldehydes, phosphorus ylides, and propargyl azide is reported. The reaction sequence involves a Wittig reaction, a Staudinger reaction, an aza-Wittig reaction, a 6π-3-azatriene electrocyclization, and a 1,3-H shift. This protocol provides quick access to the polysubstituted pyridines from readily available substrates in good to excellent yields.

Synthesis of MC 903, a biologically active vitamin D metabolite analogue

Calverley

, p. 4609 - 4619,4609-4619 (2007/10/02)

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